Minseok Kwak

Prof. Dr. Minseok Kwak

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Research Focus & Metrics

Academic Career Length

20Years (2007-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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1 January 2011 in Chemical Society Reviews
Verified
Journal Article
Closed access
MKMinseok Kwak
Minseok Kwak
AHAndreas Herrmann
Andreas Herrmann
This review provides an overview of a relatively new class of bio-conjugates, DNA amphiphiles, which consist of oligonucleotides covalently bonded to synthetic hydrophobic units. The reader will find the basic principles for the structural design and preparation methods of the materials. Moreover, the self-assembly into superstructures of higher order will be highlighted. Finally, some potential applications will be described.

15 November 2012 in Nucleic Acids Research
Verified
Journal Article
Open access
PDF file
CLChenxiang Lin
Chenxiang Lin
SPSteven D. Perrault
Steven D. Perrault
MKMinseok Kwak
Minseok Kwak
FGFranziska Graf
Franziska Graf
WSWilliam M. Shih
William M. Shih
Most previously reported methods for purifying DNA-origami nanostructures rely on agarose-gel electrophoresis (AGE) for separation. Although AGE is routinely used to yield 0.1–1 µg purified DNA nanostructures, obtaining >100 µg of purified DNA-origami structure through AGE is typically laborious because of the post-electrophoresis extraction, desalting and concentration steps. Here, we present a readily scalable purification approach utilizing rate-zonal centrifugation, which provides comparable separation resolution as AGE. The DNA nanostructures remain in aqueous solution throughout the purification process. Therefore, the desired products are easily recovered with consistently high yield (40–80%) and without contaminants such as residual agarose gel or DNA intercalating dyes. Seven distinct three-dimensional DNA-origami constructs were purified at the scale of 0.1–100 µg (final yield) per centrifuge tube, showing the versatility of this method. Given the commercially available equipment for gradient mixing and fraction collection, this method should be amenable to automation and further scale up for preparation of larger amounts (e.g. milligram quantities) of DNA nanostructures.

15 September 2010 in Angewandte Chemie International Edition
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Journal Article
Closed access
PDF file
MKMinseok Kwak
Minseok Kwak
AHAndreas Herrmann
Andreas Herrmann

19 May 2010 in Journal of the American Chemical Society
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Journal Article
Closed access
MKMinseok Kwak
Minseok Kwak
IMInge J. Minten
Inge J. Minten
DADiana-Milena Anaya
Diana-Milena Anaya
AMAndrew J. Musser
Andrew J. Musser
MBMelanie Brasch
Melanie Brasch
AHAndreas Herrmann
Andreas Herrmann

3 February 2015 in Bioprocess and Biosystems Engineering
Verified
Journal Article
Closed access
PDF file
MPManivasagan Panchanathan
Manivasagan Panchanathan
MAMoch Syaiful Alam
Moch Syaiful Alam
KKKyong-Hwa Kang
Kyong-Hwa Kang
MKMinseok Kwak
Minseok Kwak
Se-Kwon KimSe-Kwon Kim
Se-Kwon Kim

1 March 2018 in Biomaterials
Verified
Journal Article
Closed access
JVJan Willem de Vries
Jan Willem de Vries
Sven SchnichelsSven Schnichels
Sven Schnichels
JHJosé Hurst
José Hurst
LSLisa Strudel
Lisa Strudel
AGAgnieszka Gruszka
Agnieszka Gruszka
AHAndreas Herrmann
Andreas Herrmann